genome reference consortium human build 38 patch release 14 Search Results


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ATCC human lung fibroblasts
FIGURE 2. Subcellular localization of RB during cell cycle progression. WI-38 normal human lung <t>fibroblasts</t> (upper two panels) and Cdk4WT normal MEFs (middle three panels) and Cdk4R/R cells (lower three panels) were synchronized in G0-phase by 0.1% serum starvation for 72 h. Cells were stimulated to enter the cell cycle upon incubation in media containing 10% fetal bovine serum and cell preparations at indicated time points after serum starvation and after serum stimulation were subjected to immunofluorescence analysis using anti-RB (G3–245 clone) antibody and anti-phospho RB807/811 antibodies (p-RB). RB (red), phospho RB807/811(green), and DAPI (blue) images are shown. Percentage of cells with nuclear (N) and nucleocytoplasmic (NC) localization of RB and p-RB is indicated in the upper right corner of each panel.
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FIGURE 2. Subcellular localization of RB during cell cycle progression. WI-38 normal human lung <t>fibroblasts</t> (upper two panels) and Cdk4WT normal MEFs (middle three panels) and Cdk4R/R cells (lower three panels) were synchronized in G0-phase by 0.1% serum starvation for 72 h. Cells were stimulated to enter the cell cycle upon incubation in media containing 10% fetal bovine serum and cell preparations at indicated time points after serum starvation and after serum stimulation were subjected to immunofluorescence analysis using anti-RB (G3–245 clone) antibody and anti-phospho RB807/811 antibodies (p-RB). RB (red), phospho RB807/811(green), and DAPI (blue) images are shown. Percentage of cells with nuclear (N) and nucleocytoplasmic (NC) localization of RB and p-RB is indicated in the upper right corner of each panel.
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FIGURE 2. Subcellular localization of RB during cell cycle progression. WI-38 normal human lung <t>fibroblasts</t> (upper two panels) and Cdk4WT normal MEFs (middle three panels) and Cdk4R/R cells (lower three panels) were synchronized in G0-phase by 0.1% serum starvation for 72 h. Cells were stimulated to enter the cell cycle upon incubation in media containing 10% fetal bovine serum and cell preparations at indicated time points after serum starvation and after serum stimulation were subjected to immunofluorescence analysis using anti-RB (G3–245 clone) antibody and anti-phospho RB807/811 antibodies (p-RB). RB (red), phospho RB807/811(green), and DAPI (blue) images are shown. Percentage of cells with nuclear (N) and nucleocytoplasmic (NC) localization of RB and p-RB is indicated in the upper right corner of each panel.
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FIGURE 2. Subcellular localization of RB during cell cycle progression. WI-38 normal human lung <t>fibroblasts</t> (upper two panels) and Cdk4WT normal MEFs (middle three panels) and Cdk4R/R cells (lower three panels) were synchronized in G0-phase by 0.1% serum starvation for 72 h. Cells were stimulated to enter the cell cycle upon incubation in media containing 10% fetal bovine serum and cell preparations at indicated time points after serum starvation and after serum stimulation were subjected to immunofluorescence analysis using anti-RB (G3–245 clone) antibody and anti-phospho RB807/811 antibodies (p-RB). RB (red), phospho RB807/811(green), and DAPI (blue) images are shown. Percentage of cells with nuclear (N) and nucleocytoplasmic (NC) localization of RB and p-RB is indicated in the upper right corner of each panel.
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Bacteria and the probe numbers in the microarray
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Bacteria and the probe numbers in the microarray
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Chem Impex International amphotericin b
Minimum inhibitory concentration (MIC) of rhodanine compounds against Candida albicans .
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Image Search Results


FIGURE 2. Subcellular localization of RB during cell cycle progression. WI-38 normal human lung fibroblasts (upper two panels) and Cdk4WT normal MEFs (middle three panels) and Cdk4R/R cells (lower three panels) were synchronized in G0-phase by 0.1% serum starvation for 72 h. Cells were stimulated to enter the cell cycle upon incubation in media containing 10% fetal bovine serum and cell preparations at indicated time points after serum starvation and after serum stimulation were subjected to immunofluorescence analysis using anti-RB (G3–245 clone) antibody and anti-phospho RB807/811 antibodies (p-RB). RB (red), phospho RB807/811(green), and DAPI (blue) images are shown. Percentage of cells with nuclear (N) and nucleocytoplasmic (NC) localization of RB and p-RB is indicated in the upper right corner of each panel.

Journal: Journal of Biological Chemistry

Article Title: Nucleocytoplasmic Shuttling of the Retinoblastoma Tumor Suppressor Protein via Cdk Phosphorylation-dependent Nuclear Export

doi: 10.1074/jbc.m605271200

Figure Lengend Snippet: FIGURE 2. Subcellular localization of RB during cell cycle progression. WI-38 normal human lung fibroblasts (upper two panels) and Cdk4WT normal MEFs (middle three panels) and Cdk4R/R cells (lower three panels) were synchronized in G0-phase by 0.1% serum starvation for 72 h. Cells were stimulated to enter the cell cycle upon incubation in media containing 10% fetal bovine serum and cell preparations at indicated time points after serum starvation and after serum stimulation were subjected to immunofluorescence analysis using anti-RB (G3–245 clone) antibody and anti-phospho RB807/811 antibodies (p-RB). RB (red), phospho RB807/811(green), and DAPI (blue) images are shown. Percentage of cells with nuclear (N) and nucleocytoplasmic (NC) localization of RB and p-RB is indicated in the upper right corner of each panel.

Article Snippet: Cell Culture and Drug Treatments and Plasmids—Mouse embryo fibroblasts (MEFs) (11, 12) and WI-38 normal human lung fibroblasts (passage 14; ATCC) were cultured in Dulbecco’s modified Eagle’s medium with 10% fetal bovine serum (FBS).

Techniques: Incubation, Immunofluorescence

Bacteria and the probe numbers in the microarray

Journal: Biosensors & bioelectronics

Article Title: Microarray method to monitor 40 intestinal bacterial species in the study of azo dye reduction

doi: 10.1016/j.bios.2004.04.011

Figure Lengend Snippet: Bacteria and the probe numbers in the microarray

Article Snippet: Anaerobic bacteria were cultured at 35 °C in either prereduced anaerobically sterilized (PRAS) Brain Heart Infusion (BIH) broth supplemented with vitamin K and hemin (Remel, Lenexa, KS, USA), inoculated under an oxygen-free cannula using 85% nitrogen, 10% hydrogen and 5% carbon dioxide, or on PRAS brucella blood agar plates supplemented with vitamin K and hemin (Remel). table ft1 table-wrap mode="anchored" t5 caption a7 Number Bacterial species and strain Probe number 1 B. thetaiotaomicron ATCC 29148 1, 2, 3 2 B. vulgatus ATCC 8482 4, 5, 6 3 B. fragilis ATCC 23745 7, 8, 9 4 B. distasonis ATCC 8503 10, 11, 12 5 C. clostridioforme ATCC 29084 13, 14, 15 6 C. leptum ATCC 29065 16, 17, 18 7 F. prausnitzii ATCC 27768 19, 20, 21 8 P. productus ATCC 27340 22, 23, 24 9 R. obeum ATCC 29174 25, 26, 27 10 R. bromii ATCC 27255 28, 29, 30 11 R. callidus ATCC 27760 31, 32, 33 12 R. albus ATCC 27210 34, 35, 36 13 B. longum ATCC 15707 37, 38, 39 14 B. adolescentis ATCC 15703 40, 41, 42 15 B. infantis ATCC 15697 43, 44, 45 16 E. biforme ATCC 27806 46, 47, 48 17 E. aerofaciens ATCC 25986 49, 50, 51 18 L. acidophilus ATCC 4356 52, 53, 54 19 E. coli ATCC 25922 55, 56, 57 20 E. faecium ATCC 19434 58, 59, 60 21 B. uniformis ATCC 8492 61, 62, 63 22 B. ovatus ATCC 8483 64, 65, 66 23 B. caccae ATCC 43185 67, 68, 69 24 C. perfringens ATCC 13124 70, 71, 72 25 C. butyricum ATCC 19398 73, 74, 75 26 C. ramosum ATCC 25582 76, 77, 78 27 C. difficile ATCC 9689 79, 80, 81 28 C. indolis ATCC 25771 82, 83, 84 29 F. russii ATCC 25533 85, 86, 87 30 F. nucleatum ATCC 25586 88, 89, 90 31 B. catenulatum ATCC 27539 91, 92, 93 32 B. angulatum ATCC 27535 94, 95, 96 33 E. rectale ATCC 33656 97, 98, 99 34 E. eligens ATCC 27750 100, 101, 102 35 E. limosum ATCC 8486 103, 104, 105 36 E. lentum ATCC 25553 106, 107, 108 37 L. fermentum ATCC 9338 109, 110, 111 38 E. faecalis ATCC 27274 112, 113, 114 39 P. magnus ATCC 14955 115, 116, 117 40 R. gnavus ATCC 291492 118, 119, 120 Open in a separate window Bacteria and the probe numbers in the microarray 2.2.

Techniques: Bacteria

Microarray test results read from

Journal: Biosensors & bioelectronics

Article Title: Microarray method to monitor 40 intestinal bacterial species in the study of azo dye reduction

doi: 10.1016/j.bios.2004.04.011

Figure Lengend Snippet: Microarray test results read from

Article Snippet: Anaerobic bacteria were cultured at 35 °C in either prereduced anaerobically sterilized (PRAS) Brain Heart Infusion (BIH) broth supplemented with vitamin K and hemin (Remel, Lenexa, KS, USA), inoculated under an oxygen-free cannula using 85% nitrogen, 10% hydrogen and 5% carbon dioxide, or on PRAS brucella blood agar plates supplemented with vitamin K and hemin (Remel). table ft1 table-wrap mode="anchored" t5 caption a7 Number Bacterial species and strain Probe number 1 B. thetaiotaomicron ATCC 29148 1, 2, 3 2 B. vulgatus ATCC 8482 4, 5, 6 3 B. fragilis ATCC 23745 7, 8, 9 4 B. distasonis ATCC 8503 10, 11, 12 5 C. clostridioforme ATCC 29084 13, 14, 15 6 C. leptum ATCC 29065 16, 17, 18 7 F. prausnitzii ATCC 27768 19, 20, 21 8 P. productus ATCC 27340 22, 23, 24 9 R. obeum ATCC 29174 25, 26, 27 10 R. bromii ATCC 27255 28, 29, 30 11 R. callidus ATCC 27760 31, 32, 33 12 R. albus ATCC 27210 34, 35, 36 13 B. longum ATCC 15707 37, 38, 39 14 B. adolescentis ATCC 15703 40, 41, 42 15 B. infantis ATCC 15697 43, 44, 45 16 E. biforme ATCC 27806 46, 47, 48 17 E. aerofaciens ATCC 25986 49, 50, 51 18 L. acidophilus ATCC 4356 52, 53, 54 19 E. coli ATCC 25922 55, 56, 57 20 E. faecium ATCC 19434 58, 59, 60 21 B. uniformis ATCC 8492 61, 62, 63 22 B. ovatus ATCC 8483 64, 65, 66 23 B. caccae ATCC 43185 67, 68, 69 24 C. perfringens ATCC 13124 70, 71, 72 25 C. butyricum ATCC 19398 73, 74, 75 26 C. ramosum ATCC 25582 76, 77, 78 27 C. difficile ATCC 9689 79, 80, 81 28 C. indolis ATCC 25771 82, 83, 84 29 F. russii ATCC 25533 85, 86, 87 30 F. nucleatum ATCC 25586 88, 89, 90 31 B. catenulatum ATCC 27539 91, 92, 93 32 B. angulatum ATCC 27535 94, 95, 96 33 E. rectale ATCC 33656 97, 98, 99 34 E. eligens ATCC 27750 100, 101, 102 35 E. limosum ATCC 8486 103, 104, 105 36 E. lentum ATCC 25553 106, 107, 108 37 L. fermentum ATCC 9338 109, 110, 111 38 E. faecalis ATCC 27274 112, 113, 114 39 P. magnus ATCC 14955 115, 116, 117 40 R. gnavus ATCC 291492 118, 119, 120 Open in a separate window Bacteria and the probe numbers in the microarray 2.2.

Techniques: Microarray

Azo dye (Direct Blue 15) reduction activity of 17 bacterial species in pure culture

Journal: Biosensors & bioelectronics

Article Title: Microarray method to monitor 40 intestinal bacterial species in the study of azo dye reduction

doi: 10.1016/j.bios.2004.04.011

Figure Lengend Snippet: Azo dye (Direct Blue 15) reduction activity of 17 bacterial species in pure culture

Article Snippet: Anaerobic bacteria were cultured at 35 °C in either prereduced anaerobically sterilized (PRAS) Brain Heart Infusion (BIH) broth supplemented with vitamin K and hemin (Remel, Lenexa, KS, USA), inoculated under an oxygen-free cannula using 85% nitrogen, 10% hydrogen and 5% carbon dioxide, or on PRAS brucella blood agar plates supplemented with vitamin K and hemin (Remel). table ft1 table-wrap mode="anchored" t5 caption a7 Number Bacterial species and strain Probe number 1 B. thetaiotaomicron ATCC 29148 1, 2, 3 2 B. vulgatus ATCC 8482 4, 5, 6 3 B. fragilis ATCC 23745 7, 8, 9 4 B. distasonis ATCC 8503 10, 11, 12 5 C. clostridioforme ATCC 29084 13, 14, 15 6 C. leptum ATCC 29065 16, 17, 18 7 F. prausnitzii ATCC 27768 19, 20, 21 8 P. productus ATCC 27340 22, 23, 24 9 R. obeum ATCC 29174 25, 26, 27 10 R. bromii ATCC 27255 28, 29, 30 11 R. callidus ATCC 27760 31, 32, 33 12 R. albus ATCC 27210 34, 35, 36 13 B. longum ATCC 15707 37, 38, 39 14 B. adolescentis ATCC 15703 40, 41, 42 15 B. infantis ATCC 15697 43, 44, 45 16 E. biforme ATCC 27806 46, 47, 48 17 E. aerofaciens ATCC 25986 49, 50, 51 18 L. acidophilus ATCC 4356 52, 53, 54 19 E. coli ATCC 25922 55, 56, 57 20 E. faecium ATCC 19434 58, 59, 60 21 B. uniformis ATCC 8492 61, 62, 63 22 B. ovatus ATCC 8483 64, 65, 66 23 B. caccae ATCC 43185 67, 68, 69 24 C. perfringens ATCC 13124 70, 71, 72 25 C. butyricum ATCC 19398 73, 74, 75 26 C. ramosum ATCC 25582 76, 77, 78 27 C. difficile ATCC 9689 79, 80, 81 28 C. indolis ATCC 25771 82, 83, 84 29 F. russii ATCC 25533 85, 86, 87 30 F. nucleatum ATCC 25586 88, 89, 90 31 B. catenulatum ATCC 27539 91, 92, 93 32 B. angulatum ATCC 27535 94, 95, 96 33 E. rectale ATCC 33656 97, 98, 99 34 E. eligens ATCC 27750 100, 101, 102 35 E. limosum ATCC 8486 103, 104, 105 36 E. lentum ATCC 25553 106, 107, 108 37 L. fermentum ATCC 9338 109, 110, 111 38 E. faecalis ATCC 27274 112, 113, 114 39 P. magnus ATCC 14955 115, 116, 117 40 R. gnavus ATCC 291492 118, 119, 120 Open in a separate window Bacteria and the probe numbers in the microarray 2.2.

Techniques: Activity Assay

Minimum inhibitory concentration (MIC) of rhodanine compounds against Candida albicans .

Journal: PLoS ONE

Article Title: In Vitro Antibacterial Activity of Rhodanine Derivatives against Pathogenic Clinical Isolates

doi: 10.1371/journal.pone.0164227

Figure Lengend Snippet: Minimum inhibitory concentration (MIC) of rhodanine compounds against Candida albicans .

Article Snippet: Murine macrophage (J774A.1), human keratinocytes (HaCat) and human ileocecal colorectal (HRT-18) cell lines were purchased from ATCC (Manassas, VA), vancomycin hydrochloride (Gold Biotechnology, St. Louis, MO, USA), linezolid, amphotericin B, fusidic acid (Chem-impex International, Wood Dale, IL, USA), ciprofloxacin, gentamycin (Enzo Life Sciences, Farmingdale, NY, USA), rifampicin, erythromycin (Sigma-Aldrich, St. Louis, MO, USA), oxacillin (TCI chemicals, Portland, OR, USA), fluconazole (Acros, NJ, USA), Daptomycin (Selleckchem, Houston, TX, USA) and colistin (Alfa Aesar, Ward Hill, MA, USA) were acquired from other commercial vendors.

Techniques: Concentration Assay